SKINORITA

This brand name is authorized in Nigeria.

Active ingredients

The drug SKINORITA contains a combination of these active pharmaceutical ingredients (APIs):

`1`	Urea UNII `8W8T17847W` - UREA
	Urea is a recognised hydrating agent that has been widely used topically to treat dry or damaged skin.
	Read more about Urea
`2`	Lactic acid UNII `33X04XA5AT` - LACTIC ACID, UNSPECIFIED FORM
	Read more about Lactic acid
`3`	Glycine UNII `TE7660XO1C` - GLYCINE
	Read more about Glycine
`4`	Ammonium chloride UNII `01Q9PC255D` - AMMONIUM CHLORIDE
	Read more about Ammonium chloride
`5`	Sodium chloride UNII `451W47IQ8X` - SODIUM CHLORIDE
	Sodium chloride is the principle salt involved in maintaining the osmotic tension of blood and tissues. Changes in osmotic tension influence the movement of fluids and diffusion of salts in cellular tissue.
	Read more about Sodium chloride
`6`	Potassium chloride UNII `660YQ98I10` - POTASSIUM CHLORIDE
	Potassium plays a vital physiological role in maintenance of normal electrical excitability of nerve and muscle. It is also important in the genesis and correction of imbalances of acid-base metabolism.
	Read more about Potassium chloride
`7`	Calcium lactate UNII `2URQ2N32W3` - CALCIUM LACTATE ANHYDROUS
	Calcium lactate is used as an antacid and in calcium deficiency to treat hypocalcaemia. It can be absorbed at various pHs, thus it does not need to be taken with food. Calcium lactate is an antidote for soluble fluoride ingestion¹⁶: p165 and hydrofluoric acid.
	Read more about Calcium lactate
`8`	Magnesium chloride UNII `02F3473H9O` - MAGNESIUM CHLORIDE
	Read more about Magnesium chloride
`9`	Sodium dihydrogen phosphate dihydrate UNII `5QWK665956` - SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE
	Read more about Sodium phosphate

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A4-100358	Cream	SkinoRita Cream CREAM 100g	4 NF-PP-246490 SkinoRita Cream Urea, Lactic Acid, & Glycine. Urea 12%w/w, Latic acid 6%w/w, Glycine 0.5%w/w, Ammonium chloride 0.5%w/w, Sodium Chloride 0.5%w/w, Potassium chloride 0.5%w/w, Calcium lactate 0.5%w/w, Magnesium chloride 0.3%w/w, Sodium dihydrogen phosphate dihydrate 0.5%w/w, Stearic acid 3.75%w/w, Cetyl Alcohol 1.5%w/w, Glycerin 2.0%w/w, Disodium Edetate 0.2%w/w, Vanzan NFG 0.4%w/w, Natrosol Hydoxyethyl cellulose 0.5%w/w, Steareth -21Poly 1.0%w/w, Carnavel 165 5%w/w, Euxyl K 703 Phenoxyethanol 0.5%w/w, Dimethicon 0.2%w/w, Sepinav EMT10 1.2%w/ A4-100358 Drugs DERMATOLOGICALS Imported Products 100g POM 1 1/31/2022 THE DEVON PHARMACEUTICALS COMPANY LIMITED, 15, OKE-AFA ROAD ILUPEJU MAGBORO OGUN 7030177102 info@devonpharmaceuticals.com EAST AFRICAN (INDIA) OVERSEAS, Plot No 1, Pharmacity Selaqui, Dehradun - 248011, Uttarakhand, India, India	28/03/2023

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	A4-100358

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